Vice President Regulatory Affairs

ARTO; Glasgow; On-site; GBP 90,000 - 130,000; Full time

Job summary

A leading Bio-MedTech firm in the United Kingdom is hiring a VP of Regulatory Affairs. The role involves defining the global regulatory roadmap and leading early scientific dialogue with major regulators. Ideal candidates are UK-based senior regulatory leaders with a strong background in biologics, ATMPs, and wellness technologies, ready to thrive in a fast-paced, innovative environment. This is a key role pushing the boundaries of human health and longevity.

Qualifications

• UK-based senior regulatory leader with a strong track record.
• Background in biologics, ATMPs, regenerative medicine, or wellness.
• Experience with regulatory classifications across various domains.

Responsibilities

• Own and define the global regulatory roadmap across jurisdictions.
• Lead dialogue with major regulators like MHRA, EMA, and FDA.
• Build internal regulatory frameworks and quality standards.

Skills

Regulatory strategy

Leadership

Classifications knowledge

Solutions-focused

Job description

We are supporting an innovative Bio - MedTech company operating at the intersection of advanced therapies, biologics, wellness, and digital health and they are now hiring a VP of Regulatory Affairs.

The role will be required to shape the global regulatory strategy for a fast-growing Bio-MedTech expanding across the UK, EU / Switzerland, US, Middle East and Asia. The role is ideal for a senior regulatory leader who thrives in a pioneering, fast-moving environment and wants to be part of a mission pushing the boundaries of human health and longevity.

Key Responsibilities

• Own and define the global regulatory roadmap across multiple jurisdictions
• Clarify classifications and compliant claims for novel biologics, ATMPs, wellness interventions and digital innovations
• Lead early scientific dialogue with regulators (MHRA, EMA, Swissmedic, FDA and others)
• Build the internal regulatory frameworks, quality structures and documentation standards
• Guide communications, partnerships, and clinical / wellness deployments to remain compliant

Qualifications

• UK-based senior regulatory leader
• Background in biologics, ATMPs, regenerative medicine, advanced wellness, or novel health technologies
• Experience working on boundaries between medical, biological and wellness classifications
• Someone pragmatic, solutions-focused, and comfortable building from scratch in a dynamic environment
• A strong track record leading regulatory strategy, innovation pathways, or early regulatory dialogue

If your interested, or know someone who might be, reach out to me at :

[e-mail]